Cargando…
Monoaminergic control of spinal locomotor networks in SOD1(G93A) newborn mice
Mutations in the gene that encodes Cu/Zn-superoxide dismutase (SOD1) are the cause of approximately 20% of familial forms of amyotrophic lateral sclerosis (ALS), a fatal neurodegenerative disease characterized by the progressive loss of motor neurons. While ALS symptoms appear in adulthood, spinal m...
Autores principales: | Milan, Léa, Barrière, Grégory, De Deurwaerdère, Philippe, Cazalets, Jean-René, Bertrand, Sandrine S. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4081764/ https://www.ncbi.nlm.nih.gov/pubmed/25071458 http://dx.doi.org/10.3389/fncir.2014.00077 |
Ejemplares similares
-
Multiple monoaminergic modulation of posturo-locomotor network activity in the newborn rat spinal cord
por: Beliez, Lauriane, et al.
Publicado: (2014) -
Age-Related Changes in Pre- and Postsynaptic Partners of the Cholinergic C-Boutons in Wild-Type and SOD1(G93A) Lumbar Motoneurons
por: Milan, Léa, et al.
Publicado: (2015) -
Acetylcholine and spinal locomotor networks: The insider
por: Mille, Théo, et al.
Publicado: (2021) -
Monoaminergic Mechanisms in Epilepsy May Offer Innovative Therapeutic Opportunity for Monoaminergic Multi-Target Drugs
por: Svob Strac, Dubravka, et al.
Publicado: (2016) -
Noradrenergic Modulation of Intrinsic and Synaptic Properties of Lumbar Motoneurons in the Neonatal Rat Spinal Cord
por: Tartas, Maylis, et al.
Publicado: (2010)